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Characterizing the effects of thermal treatment on human norovirus GII.4 viability using propidium monoazide combined with RT-qPCR and quality assessments in mussels

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dc.contributor.authorJeon, Eun Bi-
dc.contributor.authorChoi, Man-Seok-
dc.contributor.authorKim, Ji Yoon-
dc.contributor.authorHa, Kwang Soo-
dc.contributor.authorKwon, Ji Young-
dc.contributor.authorJeong, Sung Hyeon-
dc.contributor.authorLee, Hee Jung-
dc.contributor.authorJung, Yeoun Joong-
dc.contributor.authorHa, Ji-Hyoung-
dc.contributor.authorPark, Shin Young-
dc.date.accessioned2022-12-26T13:01:56Z-
dc.date.available2022-12-26T13:01:56Z-
dc.date.issued2020-03-
dc.identifier.issn0956-7135-
dc.identifier.issn1873-7129-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/6858-
dc.description.abstractThis study investigated the effects of thermal treatment (70, 80, and 90 degrees C for 5, 10, and 20 min) on the titers of human norovirus (HuNoV) GII.4, a dominant genotype in fresh mussels using propidium monoazide (PMA) pretreatment and real-time reverse transcription quantitative-polymerase chain reaction (RT-qPCR) and the effects of thermal treatment on mussel quality (Hunter colors and sensory properties). Reductions of > 1-log(10) for HuNoV in PMA-treated mussels required 70 degrees C for 20 min, 80 degrees C for 10 min and 90 C for 5 min. As assessed by PMA/RT-qPCR, the log(10) reduction values of HuNoV in PMA-treated samples was significantly reduced (46% or 0.27 log(10); P < 0.05) when heated to 90 degrees C for 20 min compared with non-PMA treated samples under identical conditions. Hunter color 'L'-, and 'a'- and 'b'- values significantly (P < 0.05) decreased and increased, respectively with a stepwise increase of temperature (70-90 degrees C) and duration of heat treatment (5-20 min). The results of the untrained 7-point hedonic scale of sensory evaluation revealed that mussels heated to 90 degrees C for 10 min were the best quality sample among all thermally treated mussels. The results suggest that the PMA/RT-qPCR method could be very effective in distinguishing HuNoV viability following high heat treatment for an extended duration (eg, 90 degrees C for 20 min). Based on these results, the PMA/RT-qPCR method could be very effective in assessing HuNoV viability following high-heat treatment for an extended duration (eg, 90 C for 20 min). Furthermore, our findings suggest that inactivation of HuNoV GII.4 in the bivalve molluscan shellfish may be accomplished by treatment at 70 degrees C for 20 min, 80 degrees C for 10 min, or 90 degrees C for 5 min. Among all thermal treatments, 90 degrees C for 10 min was considered the optimal cooking temperature and duration for mussels.-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleCharacterizing the effects of thermal treatment on human norovirus GII.4 viability using propidium monoazide combined with RT-qPCR and quality assessments in mussels-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.foodcont.2019.106954-
dc.identifier.scopusid2-s2.0-85073352120-
dc.identifier.wosid000500052400055-
dc.identifier.bibliographicCitationFood Control, v.109-
dc.citation.titleFood Control-
dc.citation.volume109-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusFELINE-CALICIVIRUS-
dc.subject.keywordPlusETHIDIUM MONOAZIDE-
dc.subject.keywordPlusINACTIVATION-
dc.subject.keywordPlusVIRUSES-
dc.subject.keywordPlusSHELLFISH-
dc.subject.keywordPlusOUTBREAKS-
dc.subject.keywordPlusBACTERIA-
dc.subject.keywordPlusPCR-
dc.subject.keywordAuthorHuman norovirus GII.4-
dc.subject.keywordAuthorMussel-
dc.subject.keywordAuthorThermal treatment-
dc.subject.keywordAuthorPropidium monoazide-
dc.subject.keywordAuthorRT-qPCR-
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